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. 2002 Feb;22(3):856–865. doi: 10.1128/MCB.22.3.856-865.2002

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Copyright © 2002, American Society for Microbiology

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FIG. 6. — Thiol pulldown analysis of the chromatin structure on the mouse cyclin E promoter in micrococcal nuclease-digested RB^+/+ and RB^−/− MEF lysates. (a) Cells were arrested in G₀ (−serum) and treated with either TSA or vehicle alone. The position of the nucleosomal region of the cyclin E promoter is shown, as is the designated primer set number for that region. Cntl, control. (b) Graphic representation of the results shown in panel a. See the legend to Fig. 3 for details. (c) Cells were arrested in G₀ (−serum) or induced to late G₁ (+serum). The position of the nucleosomal region of the cyclin E promoter is shown, as is the designated primer set number for that region. (d) Graphic representation of the results shown in panel c.

FIG. 6. — Thiol pulldown analysis of the chromatin structure on the mouse cyclin E promoter in micrococcal nuclease-digested RB^+/+ and RB^−/− MEF lysates. (a) Cells were arrested in G₀ (−serum) and treated with either TSA or vehicle alone. The position of the nucleosomal region of the cyclin E promoter is shown, as is the designated primer set number for that region. Cntl, control. (b) Graphic representation of the results shown in panel a. See the legend to Fig. 3 for details. (c) Cells were arrested in G₀ (−serum) or induced to late G₁ (+serum). The position of the nucleosomal region of the cyclin E promoter is shown, as is the designated primer set number for that region. (d) Graphic representation of the results shown in panel c.